Preventive treatment with liraglutide protects against development of glucose intolerance in a rat model of Wolfram syndrome.
Sci Rep · 2018
Last updated 2026-05-28In a rat model of Wolfram syndrome, early treatment with the GLP-1 drug liraglutide—started before symptoms appeared—prevented the development of glucose intolerance and improved insulin and glucagon secretion. The drug also reduced stress and inflammation in pancreatic islet cells, suggesting potential as a preventive therapy.
AI summary of the abstract below.
| Journal | Sci Rep, 2018 |
|---|---|
| Citations | 34 |
| Relative citation ratio | 1.54 |
| NIH percentile | 65 |
| Molecules | liraglutide |
| Conditions studied | Type 2 Diabetes |
Abstract
Wolfram syndrome (WS) is a rare autosomal recessive disorder caused by mutations in the WFS1 (Wolframin1) gene. The syndrome first manifests as diabetes mellitus, followed by optic nerve atrophy, deafness, and neurodegeneration. The underlying mechanism is believed to be a dysregulation of endoplasmic reticulum (ER) stress response, which ultimately leads to cellular death. Treatment with glucagon-like peptide-1 (GLP-1) receptor agonists has been shown to normalize ER stress response in several in vitro and in vivo models. Early chronic intervention with the GLP-1 receptor agonist liraglutide starting before the onset of metabolic symptoms prevented the development of glucose intolerance, improved insulin and glucagon secretion control, reduced ER stress and inflammation in Langerhans islets in Wfs1 mutant rats. Thus, treatment with GLP-1 receptor agonists might be a promising strategy as a preventive treatment for human WS patients.
Verbatim abstract via PubMed 29976929 ↗
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